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Learning can be detrimental for a parasitic wasp

Animals have evolved the capacity to learn, and the conventional view is that learning allows individuals to improve foraging decisions. The parasitoid Telenomus podisi has been shown to parasitize eggs of the exotic stink bug Halyomorpha halys at the same rate as eggs of its coevolved host, Podisus...

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Autores principales: Bertoldi, Valeria, Rondoni, Gabriele, Peri, Ezio, Conti, Eric, Brodeur, Jacques
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7987188/
https://www.ncbi.nlm.nih.gov/pubmed/33755694
http://dx.doi.org/10.1371/journal.pone.0238336
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author Bertoldi, Valeria
Rondoni, Gabriele
Peri, Ezio
Conti, Eric
Brodeur, Jacques
author_facet Bertoldi, Valeria
Rondoni, Gabriele
Peri, Ezio
Conti, Eric
Brodeur, Jacques
author_sort Bertoldi, Valeria
collection PubMed
description Animals have evolved the capacity to learn, and the conventional view is that learning allows individuals to improve foraging decisions. The parasitoid Telenomus podisi has been shown to parasitize eggs of the exotic stink bug Halyomorpha halys at the same rate as eggs of its coevolved host, Podisus maculiventris, but the parasitoid cannot complete its development in the exotic species. We hypothesized that T. podisi learns to exploit cues from this non-coevolved species, thereby increasing unsuccessful parasitism rates. We conducted bioassays to compare the responses of naïve vs. experienced parasitoids on chemical footprints left by one of the two host species. Both naïve and experienced females showed a higher response to footprints of P. maculiventris than of H. halys. Furthermore, parasitoids that gained an experience on H. halys significantly increased their residence time within the arena and the frequency of re-encounter with the area contaminated by chemical cues. Hence, our study describes detrimental learning where a parasitoid learns to associate chemical cues from an unsuitable host, potentially re-enforcing a reproductive cul-de-sac (evolutionary trap). Maladaptive learning in the T. podisi—H. halys association could have consequences for population dynamics of sympatric native and exotic host species.
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spelling pubmed-79871882021-04-02 Learning can be detrimental for a parasitic wasp Bertoldi, Valeria Rondoni, Gabriele Peri, Ezio Conti, Eric Brodeur, Jacques PLoS One Research Article Animals have evolved the capacity to learn, and the conventional view is that learning allows individuals to improve foraging decisions. The parasitoid Telenomus podisi has been shown to parasitize eggs of the exotic stink bug Halyomorpha halys at the same rate as eggs of its coevolved host, Podisus maculiventris, but the parasitoid cannot complete its development in the exotic species. We hypothesized that T. podisi learns to exploit cues from this non-coevolved species, thereby increasing unsuccessful parasitism rates. We conducted bioassays to compare the responses of naïve vs. experienced parasitoids on chemical footprints left by one of the two host species. Both naïve and experienced females showed a higher response to footprints of P. maculiventris than of H. halys. Furthermore, parasitoids that gained an experience on H. halys significantly increased their residence time within the arena and the frequency of re-encounter with the area contaminated by chemical cues. Hence, our study describes detrimental learning where a parasitoid learns to associate chemical cues from an unsuitable host, potentially re-enforcing a reproductive cul-de-sac (evolutionary trap). Maladaptive learning in the T. podisi—H. halys association could have consequences for population dynamics of sympatric native and exotic host species. Public Library of Science 2021-03-23 /pmc/articles/PMC7987188/ /pubmed/33755694 http://dx.doi.org/10.1371/journal.pone.0238336 Text en © 2021 Bertoldi et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Bertoldi, Valeria
Rondoni, Gabriele
Peri, Ezio
Conti, Eric
Brodeur, Jacques
Learning can be detrimental for a parasitic wasp
title Learning can be detrimental for a parasitic wasp
title_full Learning can be detrimental for a parasitic wasp
title_fullStr Learning can be detrimental for a parasitic wasp
title_full_unstemmed Learning can be detrimental for a parasitic wasp
title_short Learning can be detrimental for a parasitic wasp
title_sort learning can be detrimental for a parasitic wasp
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7987188/
https://www.ncbi.nlm.nih.gov/pubmed/33755694
http://dx.doi.org/10.1371/journal.pone.0238336
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